DO_rare_slim NCIthesaurus has material basis in has symptom disease has feature autosomal recessive disease blood coagulation disease factor VII deficiency ORDO:327 MIM:227500 MIM:227500 UMLS_CUI:C0015503 NCI:C131631 disease_ontology MESH:D005168 SNOMEDCT_US_2025_09_01:154820003 GARD:2238 ICD10CM:D68.2 DOID:2215 ORDO:327 A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade. deficiency, stable hemarthrosis autosomal recessive inheritance bleeding epistaxis gum bleeding menorrhagia